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23 Possible Causes for Hirsutism, Kallmann Syndrome, Umbilical Plaque

  • Lytic Bone Lesion

    , see ophthalmo-acromelic syndrome anosmic hypogonadism, see Kallmann syndrome anosmic idiopathic hypogonadotropic hypogonadism, see Kallmann syndrome ANS, see ataxia neuropathy[mygenomics.com] SFPKS was first described in a 5-year-old female with a distinct facial appearance, proportional short stature, hirsutism, polycystic kidneys, vertebral abnormalities, elongated[nature.com] hypertrichosis / Increased body hair - Hyperextensible joints / articular hyperlaxity - Hypoplastic mandibula / partial absence of the mandibula - Macrocephaly / macrocrania[csbg.cnb.csic.es]

  • Hypertrichotic Osteochondrodysplasia

    […] abnormalities, see Woodhouse-Sakati syndrome hypogonadotropic hypogonadism and anosmia, see Kallmann syndrome hypogonadotropic hypogonadism-anosmia syndrome, see Kallmann[herenciageneticayenfermedad.blogspot.com] Hirsutism of the lower back (B) and forearms(C) Figure 3 All images are from a woman age 40 years.[ncbi.nlm.nih.gov] SYNDROME 1; KAL1 KAL1 chrX:8,456,916-8,660,227 8,456,916 8,660,227 203,311 Xp22 #309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7 HCCS gene (300056) chrX:11,039,373-11,051,122[ngrl.org.uk]

  • Marshall-Smith Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] Individuals may also have heart defects, an increased amount of body hair (hirsutism), and flat feet (pes planus). 0005616 Anteverted nares Nasal tip, upturned Upturned nasal[rarediseases.info.nih.gov] 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18[books.google.com]

  • Hypertelorism

    Genet. (1990) [ Pubmed ] A case of Kallmann syndrome associated with Dandy-Walker malformation. Ueno, H., Yamaguchi, H., Katakami, H., Matsukura, S. Exp. Clin.[wikigenes.org]

  • Progeroid Syndrome Type Petty

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] Everted lower lip vermilion Drooping lower lip Outward turned lower lip [ more ] 0000232 Failure to thrive Faltering weight Weight faltering [ more ] 0001508 Generalized hirsutism[rarediseases.info.nih.gov] Mild hirsutism extended down her back.[docslide.net]

  • Robinow Syndrome

    ) FGFR1 ( Pfeiffer syndrome, KAL2 Kallmann syndrome ) FGFR2 ( Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome ) FGFR3[en.wikipedia.org] Note the hirsutism, bushy eyebrows, downward slanting palpebral fissures, and micrognathia. Figure 3.14.[americorpshealth.biz] […] retardation, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism[icd10data.com]

  • Kasznica-Carlson-Coppedge Syndrome

    Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome Karak Syndrome[rgd.mcw.edu] Genoa Syndrome German Syndrome Gerstmann syndrome Ghose Sachdev Kumar Syndrome Giacheti Syndrome Gilles de la Tourette syndrome Gillespie Syndrome Gingival Fibromatosis with Hypertrichosis[rgd.mcw.edu] Spastic Paraplegia Epilepsy Mental Retardation Spastic Paraplegia with Kallmann Syndrome Spastic Paraplegia, Ataxia, and Mental Retardation SPASTIC PARAPLEGIA, INTELLECTUAL[rgd.mcw.edu]

  • Simpson Dysmorphia Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] […] dysplasia Sebaceous gland hyperplasia, familial presenile Pentosuria Xanthinuria type 2 Renal hypomagnesemia-6 Deafness, autosomal dominant nonsyndromic sensorineural 3 Hypertrichosis[checkrare.com] Cardiofaciocutaneous syndrome Cataract-ataxia-deafness syndrome Cataract-congenital heart disease-neural tube defect syndrome Cataract-deafness-hypogonadism syndrome Cataract-hypertrichosis-intellectual[se-atlas.de]

  • Kniest Dysplasia

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] The baby also had significant hirsutism though there was no cleft palate (Figure 1 and 2).[jpma.org.pk] 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18[books.google.com]

  • Weaver Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.de] Additional features include hirsutism and an umbilical hernia. Hearing loss can sometimes occur.[marshallsmith.org] Respiratory disorders, hypertrichosis, and early death uniquely characterize the marshall-smith syndrome.[icd10data.com]

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